首页> 外文期刊>American journal of medical genetics, Part A >Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry
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Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry

机译:非洲血统较高的巴西人口中非综合征性唇裂伴或不伴left裂的遗传危险因素

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Nonsyndromic cleft lip with or without cleft palate (NSCL +/- P) is the most common orofacial birth defect, exhibiting variable prevalence around the world, often attributed to ethnic and environmental differences. Linkage analyses and genome-wide association studies have identified several genomic susceptibility regions for NSCL +/- P, mostly in European-derived or Asian populations. Genetic predisposition to NSCL +/- P is ethnicity-dependent, and the genetic basis of susceptibility to NSCL +/- P likely varies among populations. The population of Brazil is highly admixed, with highly variable ancestry; thus, the genetic determinants of NSCL +/- P susceptibility may be quite different. This study tested association of 8 single-nucleotide polymorphisms (SNPs), previously identified by genome-wide studies in other populations, with NSCL +/- P in a Brazilian population with high African ancestry. SNPs rs560426, rs642961, rs1530300, rs987525, rs3758249, rs7078160, rs17085106, and rs13041247 were genotyped in 293 Brazilian patients with NSCL +/- P and 352 unaffected Brazilian controls. Each sample was also genotyped for 40 biallelic short insertion/deletion polymorphic markers to characterize genetic ancestry. The average African ancestry background was 31.1% for the NSCL +/- P group and 36.7% for the control group. After adjustment for ancestry and multiple testing, the minor alleles of rs3758249 (OR: 1.58, 95% CI: 1.25-2.01, P=0.0001) and rs7078160 (OR: 1.59, 95% CI: 1.21-2.07, P=0.0002) were significantly associated with risk of NSCL +/- P. Polymorphisms located in IRF6 (rs642961) and 8q24 (rs1530300 and rs987525) showed marginal associations in this Brazilian population with high African ancestry. These results indicate that rs3758249 at 9q22 and rs7078160 at 10q25.3 represent risk loci for NSCL +/- P in the Brazilian population with high African ancestry. (c) 2015 Wiley Periodicals, Inc.
机译:非综合征性唇裂伴或不伴c裂(NSCL +/- P)是最常见的口面部先天性缺陷,在世界范围内患病率普遍不同,通常归因于种族和环境差异。连锁分析和全基因组关联研究确定了NSCL +/- P的几个基因组易感性区域,主要在欧洲或亚洲人群中。 NSCL +/- P的遗传易感性是种族依赖性的,NSCL +/- P易感性的遗传基础可能在人群中有所不同。巴西的人口高度混杂,世袭千差万别;因此,NSCL +/- P敏感性的遗传决定因素可能完全不同。这项研究测试了先前在其他人群中进行的全基因组研究确定的8个单核苷酸多态性(SNP)与非洲高血统的巴西人群中NSCL +/- P的关联。在293名巴西NSCL +/- P患者和352例未受影响的巴西对照患者中对SNP rs560426,rs642961,rs1530300,rs987525,rs3758249,rs7078160,rs17085106和rs13041247进行了基因分型。还对每个样品进行了40个双等位基因短插入/缺失多态性标记的基因分型,以表征遗传血统。 NSCL +/- P组的平均非洲血统背景为31.1%,对照组为36.7%。经过血统调整和多重检测后,rs3758249(OR:1.58,95%CI:1.25-2.01,P = 0.0001)和rs7078160(OR:1.59,95%CI:1.21-2.07,P = 0.0002)的次要等位基因为与NSCL +/- P的风险显着相关。位于IRF6(rs642961)和8q24(rs1530300和rs987525)的多态性显示,该巴西人群具有较高的非洲血统。这些结果表明,在具有较高非洲血统的巴西人口中,位于9q22的rs3758249和位于10q25.3的rs7078160代表NSCL +/- P的风险基因座。 (c)2015年威利期刊有限公司

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